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SEED HAEMATOLOGY

The importance of reticulocyte detection

Production of reticulocytes

History

All blood cells emanate from a stem cell. Under pronounced

n 
1865

proliferation they differentiate into cells of the three blood

cell lines (erythropoiesis, granulopoiesis and thrombopoiesis). Focusing on the red blood cell (RBC) line, we see that
the life span of circulating erythrocytes is approx. 120 days.
Nearly 1% of this total is lost daily and is replenished by new
cells. Every second, about two millions of RBC are being
produced. In the bone marrow the young erythroblasts eject
their cell nucleus, becoming reticulocytes which then enter
the peripheral bloodstream.

First description of reticulocytes by Erb, who

discovered an intracellular reticulum using picric acid.

n 
1881

Using supravital staining, Ehrlich demonstrated

an intracellular network that was described as substantia reticulo-filamentosa.

n 
1891

Smith identified reticulocytes as immature red

blood cells.
n 1932

Classification of maturation stages by

Heilmeyer (see Table 1).

n 
1953

Seip quantifies the maturation stages with

reference ranges (see Table 1).

As a rule, the reticulocyte remains in the bone marrow for

n 
1960

Counting of reticulocytes with methods based

a further three days and for one day in the peripheral blood-

on fluorescence (acridine orange), developed by

stream. The name reticulocyte originates from the web-like

Kosenov & Mai.

structure (reticulum in Latin), which becomes visible after

n 
1983

Tanke automates the measurement of reticulo-

staining with supravital stains, such as brilliant cresyl blue

cytes by using the fluorescence method and flow

or new methylene blue (precipitation of ribonucleic acid

cytometry.

fragments; Fig. 1). By removing the endoplasmic reticulum,

the reticulocyte develops into a mature red blood cell
within four days.

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Table 1 Maturation stages according to Heilmeyer and quantification according to Seip

Maturation stages according
to Heilmeyer

Morphological description

Quantification according to Seip

(normal %)

Stage 0

Nucleus

Stage I

Reticulum consists of dense clots

<0.1

Stage II

Loosely arranged reticulum

7.0

Stage III

Diffusely arranged reticulum

32.0

Stage IV

Some scattered granulae

61.0

The maturation stages I and IV are often interpreted incor-

If erythropoiesis is stimulated, the earlier level of matura-

rectly: stage I is sometimes described as an erythroblast and

tion shifts into the peripheral blood (similar to a left shift

stage IV as a mature RBC as its low content of RNA is not

in granulopoiesis).

detected. The correct interpretation of stage IV is especially

important, as this maturation stage is dominant in the

Reticulocyte count

peripheral bloodstream.

The normal fraction of reticulocytes in the blood depends

on the clinical situation but is usually 0.5% to 1.5% in adults

In 1986 the National Committee for Clinical Laboratory

[3] and 2% to 6% in newborns [4]. The number of reticulo-

Standards (NCCLS) classified as a reticulocyte any non-

cytes is a good indicator of bone marrow activity because it

nucleated red cell containing two or more particles of blue

represents recent production and shows the erythropoietic

stained material corresponding to ribosomal RNA [1]. The

status of the patient and if the production is healthy or not.

International Council for Standardization in Haematology

Therefore, a reliable count of the reticulocytes is needed.

(ICSH) also accepted this definition [2].

A comparison of different reference ranges as reported by

different authors can be found in a review article published
by Piva et al. [5]

Indications for counting reticulocytes

n

Basic diagnostic work-up in all types of anaemias

Therapeutic monitoring during iron, vitamin B12

or folate replacement

Therapeutic monitoring under erythropoietin

treatment

Fig. 1 Supravital stain of a smear of human blood with different stages

of reticulocytes

Monitoring during stem cell transplantation

Newborns and paediatric patients

The reticulocytes reflect the regeneration of erythropoiesis.

Determining reticulocytes from EDTA blood remains reliable

In a balanced system, >90% of the very mature stages of

for up to 72 hours after blood sampling. The storage temper-

reticulocytes (stages III and IV) are present in the peripheral

ature of +4 C or 20 C, respectively, has no significant effect

bloodstream.

on the measured result [6].

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Manual count
(Materials: supravital stains, such as brilliant cresyl blue

level of reproducibility of the results. In automated counts

or new methylene blue, a prepared microscope slide and

the measurement signals of up to 30,000 red blood cells are

a microscope).

evaluated. This results in both high count rates and a high

1. Whole blood is mixed with equal volumes of a supravital

degree of precision. Compared to manual reticulocyte

stain.

counting, automated counting results (Fig. 2) are available

2. After incubation the sample is smeared on a microscope

much faster, actually in less than one minute.

slide and air-dried.

immersion magnification (1,000-fold magnification).
4. 1,000 red blood cells are counted. At 1,000-fold magnification this corresponds to approx. five visual fields, each
consisting of approx. 200 red cells.

Forward scatter

3. The reticulocytes are counted under the microscope at oil

5. Reticulocyte counts are given per mill [] or per

cent [%].
Error rates for manual counting are quoted in the literature
at 2550% CV [78] and higher, depending on the number
of reticulocytes. Counting 1,000 cells is recommended
as standard. According to a recommendation by the ICSH
(1998) [9] on the counting rate in the reference range
of reticulocytes, at least 40,000 cells should be counted
to avoid exceeding a statistical error of 5% (Table 2).
Table 2 Effect of the number of counted RBC on the statistical error
in reticulocyte counts. The numbers quoted refer to a CV of 5%.

Fluorescence
Fig. 2 Scattergram of the reticulocyte channel (RBC: mature red blood
cells; RET: reticulocytes; PLT: fluorescence-optical platelets)

Reticulocyte count
in blood (%)

Number of cells to be counted

to achieve a CV of 5%

Reticulocyte count in the clinical diagnosis

39,600

The interpretation of the reticulocyte count is problematic

19,600

in severe anaemias. A moderately increased relative reticu-

7,600

10

3,600

20

1,600

50

400

locyte count in severe anaemia does not indicate a sufficiently strong regeneration of erythropoiesis, but merely
indicates a shortened life span of the red blood cells. It is
preferable to report the absolute reticulocyte concentration
as reticulocytes/L, as this provides a direct measurement
of erythropoietic performance.

Automated counting
To accurately measure reticulocyte counts, automated counters

For example, a value of 20 reticulocytes is considered

use a combination of laser excitation, detectors and a fluo-

increased. However, in severe anaemia with 2 million red

rescence marker that labels RNA and DNA (such as thiazole

blood cells, 20 reticulocytes merely represent 40,000

orange or polymethines) [10].

reticulocytes/L, a value within the reference range.

To measure the reticulocytes, the sample is incubated with

The relative number of reticulocytes ( and %) gives

an RNA-binding fluorescence marker and counted by flow

some information about the life span of the red blood cells,

cytometry. Automated reticulocyte counters use objective

whereas their cell concentration (reticulocytes/ L) reflects

thresholds for the classification of cells. This ensures a high

the erythropoietic productivity of the bone marrow.

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should increase within 23 days in response to the loss of

With a simple formula, relative counts (%) can be

RBC, and reach its peak in 610 days [11]. If that does not

converted into cell concentrations (RET/L):

happen, it could point out a defect of the erythropoietic

RET [%] x RBC [106/L]

= reticulocyte concentration [106/L]
100

process in the bone marrow.

In case of a pronounced red blood cell production, the mat-

The reference ranges in percentage and absolute

uration of the reticulocytes shifts into the peripheral blood

of reticulocytes according to Cavill et al. [6] are the

as the reticulocytes are passed into peripheral blood at an

following:

earlier stage (the altered dwell time in peripheral blood is

Relative reticulocytes:

m/f 0.43 1.36%

Reticulocyte count:

f 17.0 63.8 x 109/L

m 23.0 70.1 x 109/L

called a shift). This leads to a pronounced increase in circulating reticulocytes, but does not represent proof of erythropoietic performance. The maturation time of reticulocytes
in bone marrow is proportional to the haematocrit, i.e. it

It is necessary to remember that published reference ranges

decreases with the haematocrit, and the maturation time

from other analysers may be used on newer analysers, but

in peripheral blood increases. To give an indication of the

only after having validated them. Since there are also differ-

efficiency of the bone marrow, the reticulocyte count is

ences between haematological reference intervals from dif-

corrected by this haematocrit-dependent factor.

ferent populations, every lab will need to select which of the

published reference ranges fits better their own population.

Reticulocyte-associated parameters
Reticulocyte index (RI)
The relative portion ( and %) of reticulocytes may
increase, if either the reticulocytes are in fact increased or
the red blood cells are decreased. Corrective measures can
be carried out via the patients haematocrit by reference
to a normal haematocrit of 0.45 [L/L]. This type of correction

Table 3 Link between haematocrit and maturation time of reticulocytes

in peripheral blood
Haematocrit

Reticulocyte survival in blood

= maturation correction

3645%

1 day

2635%

1.5 days

1625%

2 days

15% and below

2.5 days

is recommended with anaemias:

The RPI should be between 0.5% and 2.5% for a healthy
RI = RET [%] x HCT [L/L]
0.45 [L/L] (standard HCT)

individual [11]. In case of anaemia, an RPI <2% indicates

inadequate production of reticulocytes, while an RPI >3%
indicates compensatory production of reticulocytes to

Reticulocyte production index (RPI)

replace the lost red blood cells [12].

The RPI is an index, which helps to evaluate erythropoiesis

efficiency and thus the productivity of the bone marrow. The
physiological maturation of reticulocytes is divided into the
bone marrow maturation (about 810 days since the first

RPI =

division of the proerythroblast) and about 12 days in

the peripheral blood stream until they become mature red
blood cells.

Example:
Patient values: HCT= 0.25 L/L, reticulocytes = 20

The idea of the RPI is to assess whether the bone marrow

is producing an appropriate response to an anaemic state.
After an acute haemorrhage, the reticulocyte production

RET [%]
HCT [L/L] (patient)
x
RET maturation time
0.45 (standard HCT)
in blood in days

RPI =

20 [%]
x
2

0.25
0.45

= 5.5

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Immature Reticulocyte Fraction (IRF)

Reticulocyte maturation

The IRF value is an early marker for evaluating the regeneration

In addition to conventional reticulocyte measurement, the

of erythropoiesis. Whereas the IRF percentage increases after

fluorescence flow cytometry method allows the classifica-

only a few hours, the reticulocyte count increases after 23

tion of reticulocytes into three maturation stages. These

days. If the IRF value does not increase during the treatment

maturation stages are defined by the RNA content of the

of deficiency anaemias with erythropoietin or vitamins, this

reticulocyte, measured on the analyser as fluorescence

indicates a lack of response to therapy. In addition, it helps to

intensity. The higher the RNA content, the less mature the

classify hypo-, normo- and hyper-regenerative anaemias.

reticulocytes are.

Together, the IRF value and the reticulocyte count have

Reticulocytes are fractioned according to their fluorescence

proven themselves as monitoring parameters for bone mar-

intensity into the following three categories representing

row and stem cell transplants. With successful transplants,

different maturity stages (Table 4):

in 80% of the cases the IRF value reaches its 5% mark earlier

than the granulocytes their classic threshold of 0.5 x 109

LFR (low-fluorescence reticulocytes)

mature reticulocytes

granulocytes/L [13].

MFR (medium-fluorescence reticulocytes)

An example of this utility can be seen in Fig. 3, where differ-

n HFR

semi-mature reticulocytes
ent pathologies are represented with different levels of

(high-fluorescence reticulocytes)

immature reticulocytes

immature and mature reticulocytes. As an example, in the

case of aplasia, both immature (IRF) and total reticulocytes

IRF is the sum of MFR plus HFR, i.e. the immature

are low. This type of anaemia affects the precursors of red

reticulocytes, and is also referred to as the reticulocyte

blood cells but not the ones of the white blood cell line.

maturation index.

The bone marrow ceases to produce red blood cells, and

IRF = MFR + HFR

that is why neither immature nor mature reticulocytes can

be observed.
The reference range [14] of IRF is 1.610.5%, for both men
and women.

Immature
reticulocytes

Acute
leukaemia

Haemolysis

High
Dyserythropoiesis
Normal

Low

Polycyth.
vera

Normal

Aplasia

Low

Fig. 4 Scattergram of the reticulocyte channel

Normal

High

Fig. 3 The importance of reticulocytes for clinical diagnosis

Reticulocytes

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Table 4 Maturation stages of reticulocytes

LFR

MFR

HFR

Low-Fluorescence Reticulocytes

Medium-Fluorescence Reticulocytes

High-Fluorescence Reticulocytes

Little content of RNA

Medium content of RNA

High content of RNA

Mature reticulocytes

Semi-mature reticulocytes

Immature reticulocytes

Reference range: 86.598.5%

Reference range: 1.511.5%

Reference range: 01.4%

Reticulocyte Haemoglobin equivalent (RET-He)

In addition to the quantitative determination of the blood
count parameters (RBC, HGB, RET#/%, IRF, MCV), RET-He

Indication
n

anaemias

offers a qualitative dimension. Red blood cells have a 120-day

lifetime. Therefore, using them for detecting iron deficiencies

to erythropoiesis.

Monitoring erythropoietin therapy and iron

substitution

RET-He represents the HGB content of young RBC, the reticulocytes, and thus offers real-time information on iron supply

Monitoring the therapy of chronic infections or

tumours

and changes in the iron status of erythropoiesis is only

possible at a relatively late point in time. In contrast to that,

Classification of normochromic and hypochromic

Determining the trend of the current iron status

Early marker for diseases. Together with RET#, it lets

clinicians draw conclusions on both the quality and

Measuring the haemoglobin content of the reticulocytes

quantity of the young RBC fraction.

means you can look at the current iron supply to erythropoiesis and judge the quality of the newly produced cells.

The reference ranges of RET-He [14] are (for both men

This lets you detect changes in iron status far earlier than

and women) 1,9962,407 fmol or 32.138.8 pg.

through the haemoglobin content of mature red blood cells.

The determination of RET-He can be performed on the
haematology analyser together with the routine parameters

RET-He alone provides information on the current bioavaila-

obtained during the whole blood test. A major advantage

bility of iron a low value means there is a lack of iron or

over the parameters ferritin or transferrin is that RET-He is

iron is not bioavailable for erythropoiesis. It is often used

not affected by the acute phase reaction. These conventional

together with ferritin a high or normal ferritin value

biochemical markers are drastically disturbed e.g. during

together with a low RET-He value can suggest functional

inflammation, pregnancy, or in the presence of many other

iron deficiency while low ferritin values together with a low

severe diseases, so that a clinical interpretation of the

RET-He suggest a classic iron deficiency. Since ferritin is

results would then be difficult or impossible. Measuring the

falsely increased during the acute phase of diseases, pres-

haemoglobin content of the reticulocytes as a direct assess-

ence of inflammation should be checked, e.g. by CRP.

ment of the iron actually used for the biosynthesis of haemoglobin can indicate even in these cases whether there is

RET-He is used for monitoring erythropoietin (EPO) and/

enough iron available for erythropoiesis.

or IV iron therapy. If the value increases it indicates the

therapy is having a positive effect.

The clinical usefulness of the RET-He parameter has been

proven and it is now an established parameter in advanced
haematological analysis.

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Thomas-Plot index

Thomas plot can also be used to monitor the patients that

In 2006, Thomas et al. described a diagnostic plot model in

are under treatment and see how they move from one quad-

order to differentiate iron-deficient states and predict those

rant to another.

patients who will respond to erythropoietin therapy [15].

The balance of the iron in our body is regulated by the rate

Conclusions

of erythropoiesis and the size of the iron stores. The rela-

A reliable reticulocyte count including some more parameters

tionship between erythropoietic haemoglobin incorporation

associated with reticulocytes (IRF, RPI, etc.) are important to

(RET-He) and iron stores (ferritin) can be described in a

see if the bone marrow is working properly to develop new

diagnostic plot. This plot, called Thomas plot, allows the

red blood cells, but the quantity aspect is not the only one

differentiation of classical iron deficiency from anaemia of

that is important. We have seen that the reticulocyte hae-

chronic disease. The plot indicates the correlation between

moglobinisation, RET-He, is also of high importance in order

the ratio sTfR/log ferritin (ferritin index), a marker of iron

to define the quality of the newly produced reticulocytes.

supply for erythropoiesis, and the RET-He (Fig. 5) [16]. The

Reliable reticulocyte information, regarding quality and
quantity, helps in the differential diagnosis of anaemias as
well as in the monitoring of patients.

Fig. 5 Thomas plot to identify different phases of advancing

iron deficiency (ACD: anaemia of chronic disorders, ERF: end-stage
renal failure, IDA: Iron deficiency anaemia, ID: classic iron deficiency)

References
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[2] T
 he Expert Panel on Cytometry of the International Council of
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[8] 
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[14] Pekelharing et al. (2010): Haematology reference intervals for

established and novel parameters in healthy adults. Sysmex Journal
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[15] 
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[13] 
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